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C Vermeer

Showing results (161-170 of 201) with videos related to

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The Journal of Nutrition, Health & Aging|October 21, 2015
Vitamin K Status Is not Associated with Cognitive Decline in Middle Aged AdultsE G H M van den Heuvel, N M van Schoor, C Vermeer, et al.
Bone|September 30, 2004
Bone metabolism in galactosemiaB Panis, P Ph Forget, M J P G van Kroonenburgh, et al.
Chemosphere|July 20, 2000
Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin or 2,2',4,4',5,5'-hexachlorobiphenyl on vitamin K-dependent blood coagulation in male and female WAG/Rij-ratsC A Bouwman, E Van Dam, K M Fase, et al.
Journal of Thrombosis and Haemostasis : JTH|September 13, 2007
Post-translational modifications regulate matrix Gla protein function: importance for inhibition of vascular smooth muscle cell calcificationL J Schurgers, H M H Spronk, J N Skepper, et al.
Journal of Thrombosis and Haemostasis : JTH|May 16, 2014
Circulating desphospho-uncarboxylated matrix γ-carboxyglutamate protein and the risk of coronary heart disease and strokeG W Dalmeijer, Y T van der Schouw, E J Magdeleyns, et al.
BMC Primary Care|June 14, 2024
Comparing the diagnostic considerations between general practitioners with a special interest in cardiovascular disease and those without in patients with symptoms suggestive of heart failure: a vignette studyCornelia J C Vermeer, Amy Groenewegen, Monika Hollander, et al.
Journal of Thrombosis and Haemostasis : JTH|April 23, 2004
Characteristics of recombinant W501S mutated human gamma-glutamyl carboxylaseB A M Soute, D-Y Jin, H M H Spronk, et al.
Journal of Human Hypertension|May 29, 2015
Desphospho-uncarboxylated matrix Gla protein is associated with increased aortic stiffness in a general populationO Mayer, J Seidlerová, P Wohlfahrt, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 25, 2013
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7Alexa M C Vermeer, Klaartje van Engelen, Alex V Postma, et al.
The Journal of Biological Chemistry|June 27, 2001
A polymorphism of the human matrix gamma-carboxyglutamic acid protein promoter alters binding of an activating protein-1 complex and is associated with altered transcription and serum levelsA Farzaneh-Far, J D Davies, L A Braam, et al.
Pageof 21

Showing results (161-170 of 201) with videos related to

Sort By:
Pageof 21
The Journal of Nutrition, Health & Aging|October 21, 2015
Vitamin K Status Is not Associated with Cognitive Decline in Middle Aged AdultsE G H M van den Heuvel, N M van Schoor, C Vermeer, et al.
Bone|September 30, 2004
Bone metabolism in galactosemiaB Panis, P Ph Forget, M J P G van Kroonenburgh, et al.
Chemosphere|July 20, 2000
Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin or 2,2',4,4',5,5'-hexachlorobiphenyl on vitamin K-dependent blood coagulation in male and female WAG/Rij-ratsC A Bouwman, E Van Dam, K M Fase, et al.
Journal of Thrombosis and Haemostasis : JTH|September 13, 2007
Post-translational modifications regulate matrix Gla protein function: importance for inhibition of vascular smooth muscle cell calcificationL J Schurgers, H M H Spronk, J N Skepper, et al.
Journal of Thrombosis and Haemostasis : JTH|May 16, 2014
Circulating desphospho-uncarboxylated matrix γ-carboxyglutamate protein and the risk of coronary heart disease and strokeG W Dalmeijer, Y T van der Schouw, E J Magdeleyns, et al.
BMC Primary Care|June 14, 2024
Comparing the diagnostic considerations between general practitioners with a special interest in cardiovascular disease and those without in patients with symptoms suggestive of heart failure: a vignette studyCornelia J C Vermeer, Amy Groenewegen, Monika Hollander, et al.
Journal of Thrombosis and Haemostasis : JTH|April 23, 2004
Characteristics of recombinant W501S mutated human gamma-glutamyl carboxylaseB A M Soute, D-Y Jin, H M H Spronk, et al.
Journal of Human Hypertension|May 29, 2015
Desphospho-uncarboxylated matrix Gla protein is associated with increased aortic stiffness in a general populationO Mayer, J Seidlerová, P Wohlfahrt, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 25, 2013
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7Alexa M C Vermeer, Klaartje van Engelen, Alex V Postma, et al.
The Journal of Biological Chemistry|June 27, 2001
A polymorphism of the human matrix gamma-carboxyglutamic acid protein promoter alters binding of an activating protein-1 complex and is associated with altered transcription and serum levelsA Farzaneh-Far, J D Davies, L A Braam, et al.
Pageof 21